Inflammatory caspases: Targets for novel therapies

被引:101
作者
Cornelis, Sigrid
Kersse, Kristof
Festjens, Nele
Lamkanfi, Mohamed
Vandenabeele, Peter
机构
[1] Univ Ghent VIB, Dept Mol Biomed Res, B-9052 Ghent, Belgium
[2] Univ Ghent VIB, Dept Mol Biol, B-9052 Ghent, Belgium
关键词
peptide inhibitor; caspases; apoptosis; neurodegeneration; inflammation; inflammasome; autoimmune disease; pralnacasan; animal model; INTERLEUKIN-1-BETA CONVERTING-ENZYME; COLD AUTOINFLAMMATORY SYNDROME; AMYOTROPHIC-LATERAL-SCLEROSIS; COLLAGEN-INDUCED ARTHRITIS; TRANSGENIC MOUSE MODEL; MUCKLE-WELLS-SYNDROME; GAMMA-INDUCING FACTOR; RECEPTOR ANTAGONIST; CELL-DEATH; MICE DEFICIENT;
D O I
10.2174/138161207780163006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This review provides an overview of the biochemistry and activation of' inflammatory caspases, and focuses on their therapeutic potential as disease targets in pathologies such as sepsis, Crohn's disease, rheumatoid arthritis, traumatic brain injury and amyotrophic lateral sclerosis (ALS). We summarize the proof-of-principal evidence obtained by studies in several corresponding experimental disease models confirming the validity of strategies targeting inflammatory caspases. We discuss the use of inflammatory caspase inhibitors, such as VX-740 (Pralnacasan) and VX-765, in clinical studies for rheumatoid arthritis and osteoarthritis. Finally, we point out recent approaches identifying novel peptidomimetic or non-peptide caspase inhibitors with suitable clinical profiles.
引用
收藏
页码:367 / 385
页数:19
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